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Summary Anatomy Item Literature (6278) Expression Attributions Wiki
XB-ANAT-475

Papers associated with primary germ layer (and kcnj11)

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Modeling endoderm development and disease in Xenopus., Edwards NA., Curr Top Dev Biol. January 1, 2021; 145 61-90.

Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome., Adams DS., J Physiol. June 15, 2016; 594 (12): 3245-70.                              

Xenopus as a model system for studying pancreatic development and diabetes., Kofent J., Semin Cell Dev Biol. March 1, 2016; 51 106-16.  

Recessive mutations in PCBD1 cause a new type of early-onset diabetes., Simaite D., Diabetes. October 1, 2014; 63 (10): 3557-64.

A gating mutation at the internal mouth of the Kir6.2 pore is associated with DEND syndrome., Proks P., EMBO Rep. May 1, 2005; 6 (5): 470-5.

K(ATP) channel activity is required for hatching in Xenopus embryos., Cheng SM., Dev Dyn. December 1, 2002; 225 (4): 588-91.        

Mutations within the P-loop of Kir6.2 modulate the intraburst kinetics of the ATP-sensitive potassium channel., Proks P., J Gen Physiol. October 1, 2001; 118 (4): 341-53.                    

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